Couroux Patricia, Grosse Nicole, Salapatek Anne Marie, Goyal Yasmeen, Pfaar Oliver, Hohenfeld Ilja P
Inflamax Research DBA Cliantha Research, Mississauga, Ontario, Canada.
Altamira Medica AG, Zug, Switzerland.
Clin Transl Allergy. 2023 Jul;13(7):e12277. doi: 10.1002/clt2.12277.
House Dust Mite (HDM) is the most common indoor allergen triggering allergic symptoms. First-line pharmacotherapy treatment is recommended in international guidelines, while the avoidance of allergens represents a still unmet guideline principle. AM-301 is a new non-pharmacological nasal spray that creates a protective gel-like barrier on the nasal mucosa, preventing the contact with the allergens.
This randomized, open-label, 3-period crossover study assessed the efficacy and safety of AM-301. The objective was to determine whether AM-301 reduces allergic rhinitis (AR) symptoms in patients exposed to HDM allergens. Adults with confirmed Perennial Allergic Rhinitis (PAR; n = 37) were exposed to HDM allergen in a controlled Allergen Exposure Chamber before and during a treatment course of AM-301 (in six different sequences) within 3 weeks (A: One spray AM-301 per nostril/B: Two sprays AM-301 per nostril/C: no treatment). For the primary efficacy analysis, data from the total nasal symptom score (TNSS) were pooled from treatment A + B (D) and analyzed with Analysis of Covariance Model. As secondary endpoints, single time points, visits and symptoms were analyzed.
The primary endpoint (overall change in TNSS from baseline over all three visits) showed significant results (p = 0.0085). A comparable alleviation of all four symptoms (itchy nose, nasal congestion, runny nose, sneezing) by the protective layer started to emerge after 40 min and lasted up to 180 min (end of challenge). AM-301 resulted to be safe and well-tolerated.
AM-301 significantly reduced HDM-related allergic symptoms in a standardized allergen challenge. Protection was observed to last up to 180 min.
屋尘螨(HDM)是引发过敏症状最常见的室内过敏原。国际指南推荐一线药物治疗,而避免接触过敏原仍是一项尚未实现的指南原则。AM - 301是一种新型非药物鼻腔喷雾剂,可在鼻黏膜上形成一层保护性凝胶状屏障,防止与过敏原接触。
这项随机、开放标签、3期交叉研究评估了AM - 301的疗效和安全性。目的是确定AM - 301是否能减轻接触HDM过敏原患者的过敏性鼻炎(AR)症状。37名确诊为常年性过敏性鼻炎(PAR)的成年人在3周内,于AM - 301治疗疗程之前及期间(按六种不同顺序),在可控的过敏原暴露舱中接触HDM过敏原(A:每侧鼻孔喷一次AM - 301/B:每侧鼻孔喷两次AM - 301/C:不治疗)。对于主要疗效分析,将治疗A + B(D)的总鼻症状评分(TNSS)数据合并,并采用协方差分析模型进行分析。作为次要终点,对单个时间点、访视和症状进行分析。
主要终点(三次访视中TNSS相对于基线的总体变化)显示出显著结果(p = 0.0085)。保护层对所有四种症状(鼻痒、鼻塞、流涕、打喷嚏)的类似缓解在40分钟后开始出现,并持续长达180分钟(激发结束)。AM - 301结果显示安全且耐受性良好。
在标准化过敏原激发试验中,AM - 301显著减轻了与HDM相关的过敏症状。观察到保护作用持续长达180分钟。